EP 1354894 A2 20031022 - Fusion peptide of human type-1 collagen derived peptide and tat peptide, preparation thereof, and skin anti-aging cosmetic composition comprising the same
Title (en)
Fusion peptide of human type-1 collagen derived peptide and tat peptide, preparation thereof, and skin anti-aging cosmetic composition comprising the same
Title (de)
Fusionsprotein enthaltend ein von Typ-1 Kollagen abgeleitetes Peptid und ein Tat-Peptid, Verfahren zu seiner Herstellung und Kosmetikzusammensetzung, die ein solches Fusionsprotein aufweist
Title (fr)
Peptide de fusion comportant un peptide derivé de la collagène type 1 et un peptide Tat, sa preparation, et composition cosmetique anti-age comprenant ledit peptide de fusion
Publication
Application
Priority
KR 20020014063 A 20020315
Abstract (en)
The present invention relates to a fusion peptide, in which a self cell-penetrating Tat peptide having a self penetrating signal is bound to a human Type- I collagen C-terminal derived peptide, a preparation thereof, and a skin anti-aging cosmetic composition comprising the same. Since the fusion peptide, in which the Tat peptide is bound to the human Type- I collagen C-terminal derived peptide is highly stable and has a superior skin absorption capability, the present invention provides a skin anti-aging agent having superior synthesis of collagen and hyaluronic acid, anti-aging effects, and improved durability of the effects.The present invention relates to a fusion peptide, in which a self cell-penetrating Tat peptide having a self penetrating signal is bound to a human Type- I collagen C-terminal derived peptide, a preparation thereof, and a skin anti-aging cosmetic composition comprising the same. Since the fusion peptide, in which the Tat peptide is bound to the human Type- I collagen C-terminal derived peptide is highly stable and has a superior skin absorption capability, the present invention provides a skin anti-aging agent having superior synthesis of collagen and hyaluronic acid, anti-aging effects, and improved durability of the effects.
IPC 1-7
IPC 8 full level
C12P 21/02 (2006.01); A61K 8/00 (2006.01); A61K 8/65 (2006.01); A61K 8/72 (2006.01); A61Q 19/00 (2006.01); A61Q 19/08 (2006.01); C07K 1/04 (2006.01); C07K 1/06 (2006.01); C07K 7/08 (2006.01); C07K 14/16 (2006.01); C07K 14/78 (2006.01); C07K 19/00 (2006.01)
CPC (source: EP KR US)
A61K 8/65 (2013.01 - EP US); A61Q 19/08 (2013.01 - EP US); C07K 14/005 (2013.01 - EP US); C07K 14/78 (2013.01 - EP US); C07K 19/00 (2013.01 - KR); A61K 2800/57 (2013.01 - EP US); C07K 2319/00 (2013.01 - EP US); C12N 2740/16322 (2013.01 - EP US)
Designated contracting state (EPC)
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LI LU MC NL PT SE SK TR
DOCDB simple family (publication)
WO 03078470 A1 20030925; AU 2002343889 A1 20030929; EP 1354894 A2 20031022; EP 1354894 A3 20031029; JP 2003277399 A 20031002; JP 4231674 B2 20090304; KR 100753472 B1 20070831; KR 20030074999 A 20030922; US 2003185862 A1 20031002; US 7094407 B2 20060822
DOCDB simple family (application)
KR 0201616 W 20020827; AU 2002343889 A 20020827; EP 02292293 A 20020918; JP 2002287008 A 20020930; KR 20020014063 A 20020315; US 24383602 A 20020916